Table of contents


From the editors

p71 | doi:10.1038/nri2492

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Research Highlights

T-cell development: Stimulating company | PDF (190 KB)

p72 | doi:10.1038/nri2502

Dendritic cells: Coordinating motility and function | PDF (216 KB)

p73 | doi:10.1038/nri2493

In brief

T-cell development | Autoimmunity | T-cell development | PDF (133 KB)

p73 | doi:10.1038/nri2504

T-cell responses: Two for the price of one | PDF (161 KB)

p74 | doi:10.1038/nri2495

T-cell responses: Brainstorm by CD4+ T cells | PDF (205 KB)

p75 | doi:10.1038/nri2497

Lymphocyte migration: Getting to the site of action | PDF (198 KB)

p75 | doi:10.1038/nri2501

T-cell development: CD40–CD40L crosstalk in TH17-cell differentiation | PDF (151 KB)

p76 | doi:10.1038/nri2499

Dendritic cells: Tailoring T-helper-cell responses | PDF (126 KB)

p76 | doi:10.1038/nri2500

Natural killer cells: NK cells remember | PDF (146 KB)

p77 | doi:10.1038/nri2498

B cells: Living with the enemy! | PDF (202 KB)

p78 | doi:10.1038/nri2503

TopTop

Focus on: CD4+ T-cell diversity

Progress

Epigenetic control of FOXP3 expression: the key to a stable regulatory T-cell lineage?

Jochen Huehn, Julia K. Polansky & Alf Hamann

p83 | doi:10.1038/nri2474

Regulatory T (TReg) cells are crucial for immune homeostasis, and manipulation of their suppressive functions is a possible avenue for immunotherapy. Here, the authors discuss recent advances in our understanding of how the expression of forkhead box P3 (FOXP3), a TReg-cell-specifying transcription factor, is controlled at the molecular level.

Reviews

Epigenetic control of T-helper-cell differentiation

Christopher B. Wilson, Emily Rowell & Masayuki Sekimata

p91 | doi:10.1038/nri2487

Numerous lineage-specific transcription factors have been linked with T-helper-cell subset specification. But, as discussed here, epigenetic modifications at the gene regulatory elements where these factors bind can also contribute to the regulation of T-helper-cell differentiation and function.

RUNX proteins in transcription factor networks that regulate T-cell lineage choice

Amélie Collins, Dan R. Littman & Ichiro Taniuchi

p106 | doi:10.1038/nri2489

In this Review, the authors discuss how RUNX (runt-related transcription factor) proteins and other key transcription factors work together to direct T-cell lineage choice and CD4+ T-cell differentiation.

The different faces of Notch in T-helper-cell differentiation

Derk Amsen, Andrey Antov & Richard A. Flavell

p116 | doi:10.1038/nri2488

Recent research indicates that the Notch signalling pathway is important for directing T helper (TH)-cell differentiation. In this Review, the authors discuss contrasting results showing that Notch can have a role in both TH1- and TH2-cell differentiation, and highlight how this information might help to better understand the pathology of T-cell-mediated diseases.

GATA3 and the T-cell lineage: essential functions before and after T-helper-2-cell differentiation

I-Cheng Ho, Tzong-Shyuan Tai & Sung-Yun Pai

p125 | doi:10.1038/nri2476

The transcription factor GATA-binding protein 3 (GATA3) is best known as a master regulator of T-helper-2-cell differentiation. However, as part of a network of other transcription factors, GATA3 is also important in determining cell fate at earlier stages of haematopoiesis and lymphoid-cell development.

Perspective

Opinion
Regulation of T-helper-cell lineage development by osteopontin: the inside story

Harvey Cantor & Mari L. Shinohara

p137 | doi:10.1038/nri2460

Here, Harvey Cantor and Mari Shinohara propose that the secreted and intracellular isoforms of osteopontin differentially regulate the development of distinct T-helper-cell subsets and, consequently, adaptive immune responses to foreign and self antigens.

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